From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes

Metal-catalyzed reductive coupling reactions between alkenes and alkynes are a long-standing tradition as a way to create complex unsaturated building blocks of value in organic synthesis ventures. Here, we review the general synthetic approaches realized under Co-catalysis utilizing chemical reduct...

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Authors: Tóth, Balázs L.; Amos, Stephanie G. E.; Kleij, Arjan W.
Format: Article
Publication date:2024
Country:España
Institution:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repository:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2072/480089
Online Access:http://hdl.handle.net/2072/480089
https://doi.org/10.1039/D4QO02143F
Access Level:Open access
Keyword:Química
54
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author Tóth, Balázs L.
author2 Amos, Stephanie G. E.
Kleij, Arjan W.
author2_role author
author
author_browse Amos, Stephanie G. E.
Kleij, Arjan W.
Tóth, Balázs L.
author_facet Tóth, Balázs L.
Amos, Stephanie G. E.
Kleij, Arjan W.
author_role author
collection Recercat. Dipósit de la Recerca de Catalunya
description Metal-catalyzed reductive coupling reactions between alkenes and alkynes are a long-standing tradition as a way to create complex unsaturated building blocks of value in organic synthesis ventures. Here, we review the general synthetic approaches realized under Co-catalysis utilizing chemical reductants, albeit with some limitations in scope and user-friendliness. A more recent advancement shows that these reductive ene–yne coupling reactions can also be accommodated by photoredox catalysis marking a stepping stone in the area, and creating new incentives for this kind of carbon–carbon bond formation and beyond.
eu_rights_str_mv openAccess
format article
id ES_62a216d8abfe15d4c19fdec29f1ed8a1
institution Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
network_acronym_str ES
network_name_str España
oai_identifier_str oai:recercat.cat:2072/480089
publishDate 2024
publishDateSort 2024
publisher Royal Society of Chemistry
publisherStr Royal Society of Chemistry
reponame_str Recercat. Dipósit de la Recerca de Catalunya
spelling From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes Tóth, Balázs L. Amos, Stephanie G. E. Kleij, Arjan W. Química 54 Metal-catalyzed reductive coupling reactions between alkenes and alkynes are a long-standing tradition as a way to create complex unsaturated building blocks of value in organic synthesis ventures. Here, we review the general synthetic approaches realized under Co-catalysis utilizing chemical reductants, albeit with some limitations in scope and user-friendliness. A more recent advancement shows that these reductive ene–yne coupling reactions can also be accommodated by photoredox catalysis marking a stepping stone in the area, and creating new incentives for this kind of carbon–carbon bond formation and beyond. info:eu-repo/semantics/acceptedVersion Royal Society of Chemistry http://hdl.handle.net/2072/480089 https://doi.org/10.1039/D4QO02143F
spellingShingle From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
Tóth, Balázs L.
Química
54
title From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
title_full From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
title_fullStr From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
title_full_unstemmed From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
title_short From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
title_sort From conventional to dual Co/photoredox mediated reductive coupling of alkynes and alkenes
topic Química
54
topic_facet Química
54
url http://hdl.handle.net/2072/480089
https://doi.org/10.1039/D4QO02143F